GRAB recruitment by Rab27A-Rabphiln3a complex triggers Rab3A activation in human sperm exocytosis

MARÍA FLORENCIA QUEVEDO; DIEGO MARTÍN BUSTOS; MATÍAS ALBERTO BUSTOS; TOMES CLAUDIA NORA; MATÍAS ALBERTO BUSTOS; TOMES CLAUDIA NORA; DIEGO MASONE; DIEGO MASONE; MARÍA FLORENCIA QUEVEDO; DIEGO MARTÍN BUSTOS

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

ELSEVIER SCIENCE BV

Lugar: Amsterdam; Año: 2019 vol. 1866 p. 612 - 622

0167-4889

Sperm must undergo the regulated exocytosis of its dense core granule (the acrosome reaction, AR) to fertilize the egg. We have previously described that Rabs3 and 27 are organized in a RabGEF cascade within the signaling pathway elicited by exocytosis stimuli in human sperm. Here, we report the role of Rabphilin3a and GRAB, that link these secretory Rabs in the RabGEF cascade. Like Rab3 and Rab27, GRAB and Rabphilin3a are present, localize to the acrosomal region and are required for calcium-triggered exocytosis in human sperm. Sequestration of either protein with specific antibodies introduced into streptolysin O-permeabilized sperm impairs the activation of Rab3 in the acrosomal region elicited by calcium, but not that of Rab27. Biochemical and functional assays indicate that Rabphilin3a behaves as a Rab27 effector during the AR and that GRAB exhibits GEF activity toward Rab3A. Recombinant, active Rab27A pulls down Rabphilin3a and GRAB from human sperm extracts. Conversely, immobilized Rabphilin3a recruits Rab27 and GRAB; the latter promotes Rab3A activation. The enzymatic activity of GRAB toward Rab3A was also suggested by in silico and an in vitro assays with purified proteins. In summary, we describe a signaling module where Rab27A-GTP interacts with Rabphilin3a, which in turn recruits a GEF activity toward Rab3A. This is the first description of the interaction of Rabphilin3a with a GEF. Because the machinery that drives exocytosis is highly conserved, it is tempting to hypothesize that the RabGEF cascade unveiled here might be part of the molecular mechanisms that drive exocytosis in other secretory systems.